Filamentary devices having a flexible joint for treatment of vascular defects

ABSTRACT

Devices and methods for treatment of a patient&#39;s vasculature are described. Embodiments may include a permeable implant having a radially constrained state configured for delivery within a catheter lumen, an expanded state, and a plurality of elongate filaments that are woven together. The implant may include first and second permeable shells. The first permeable shell having a proximal end with a concave or recessed section and a second permeable shell having a convex section that mates with the concave or recessed section. The implant also includes a flexible, articulating joint between the first and second permeable shells.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority under 35 U.S.C. § 119(e) from U.S. Provisional Application Ser. No. 62/819,317, filed Mar. 15, 2019, which is hereby incorporated by reference in its entirety for all purposes.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable.

FIELD OF THE INVENTION

Embodiments of devices and methods herein are directed to blocking a flow of fluid through a tubular vessel or into a small interior chamber of a saccular cavity or vascular defect within a mammalian body. More specifically, embodiments herein are directed to devices and methods for treatment of a vascular defect of a patient including some embodiments directed specifically to the treatment of cerebral aneurysms of patients.

BACKGROUND

The mammalian circulatory system is comprised of a heart, which acts as a pump, and a system of blood vessels which transport the blood to various points in the body. Due to the force exerted by the flowing blood on the blood vessel the blood vessels may develop a variety of vascular defects. One common vascular defect known as an aneurysm results from the abnormal widening of the blood vessel. Typically, vascular aneurysms are formed as a result of the weakening of the wall of a blood vessel and subsequent ballooning and expansion of the vessel wall. If, for example, an aneurysm is present within an artery of the brain, and the aneurysm should burst with resulting cranial hemorrhaging, death could occur.

Surgical techniques for the treatment of cerebral aneurysms typically involve a craniotomy requiring creation of an opening in the skull of the patient through which the surgeon can insert instruments to operate directly on the patient's brain. For some surgical approaches, the brain must be retracted to expose the parent blood vessel from which the aneurysm arises. Once access to the aneurysm is gained, the surgeon places a clip across the neck of the aneurysm thereby preventing arterial blood from entering the aneurysm. Upon correct placement of the clip the aneurysm will be obliterated in a matter of minutes. Surgical techniques may be effective treatment for many aneurysms. Unfortunately, surgical techniques for treating these types of conditions include major invasive surgical procedures which often require extended periods of time under anesthesia involving high risk to the patient. Such procedures thus require that the patient be in generally good physical condition in order to be a candidate for such procedures.

Various alternative and less invasive procedures have been used to treat cerebral aneurysms without resorting to major surgery. One approach to treating aneurysms without the need for invasive surgery involves the placement of sleeves or stents into the vessel and across the region where the aneurysm occurs. Such devices maintain blood flow through the vessel while reducing blood pressure applied to the interior of the aneurysm. Certain types of stents are expanded to the proper size by inflating a balloon catheter, referred to as balloon expandable stents, while other stents are designed to elastically expand in a self-expanding manner. Some stents are covered typically with a sleeve of polymeric material called a graft to form a stent-graft. Stents and stent-grafts are generally delivered to a preselected position adjacent a vascular defect through a delivery catheter. In the treatment of cerebral aneurysms, covered stents or stent-grafts have seen very limited use due to the likelihood of inadvertent occlusion of small perforator vessels that may be near the vascular defect being treated.

In addition, current uncovered stents are generally not sufficient as a stand-alone treatment. In order for stents to fit through the microcatheters used in small cerebral blood vessels, their density is usually reduced such that when expanded there is only a small amount of stent structure bridging the aneurysm neck. Thus, they do not block enough flow to cause clotting of the blood in the aneurysm and are thus generally used in combination with vaso-occlusive devices, such as the coils discussed above, to achieve aneurysm occlusion.

Some procedures involve the delivery of embolic or filling materials into an aneurysm. The delivery of such vaso-occlusion devices or materials may be used to promote hemostasis or fill an aneurysm cavity entirely. Vaso-occlusion devices may be placed within the vasculature of the human body, typically via a catheter, either to block the flow of blood through a vessel with an aneurysm through the formation of an embolus or to form such an embolus within an aneurysm stemming from the vessel. A variety of implantable, coil-type vaso-occlusion devices are known. The coils of such devices may themselves be formed into a secondary coil shape, or any of a variety of more complex secondary shapes. Vaso-occlusive coils are commonly used to treat cerebral aneurysms but suffer from several limitations including poor packing density, compaction due to hydrodynamic pressure from blood flow, poor stability in wide-necked aneurysms, and complexity and difficulty in the deployment thereof as most aneurysm treatments with this approach require the deployment of multiple coils. Coiling is less effective at treating certain physiological conditions, such as wide neck cavities (e.g. wide neck aneurysms) because there is a greater risk of the coils migrating out of the treatment site.

A number of aneurysm neck bridging devices with defect spanning portions or regions have been attempted, however, none of these devices have had a significant measure of clinical success or usage. A major limitation in their adoption and clinical usefulness is the inability to position the defect spanning portion to assure coverage of the neck. Existing stent delivery systems that are neurovascular compatible (i.e. deliverable through a microcatheter and highly flexible) do not have the necessary rotational positioning capability. Another limitation of many aneurysm bridging devices described in the prior art is the poor flexibility. Cerebral blood vessels are tortuous, and a high degree of flexibility is required for effective delivery to most aneurysm locations in the brain.

What has been needed are devices and methods for delivery and use in small and tortuous blood vessels that can substantially block the flow of blood into an aneurysm, such as a cerebral aneurysm, with a decreased risk of inadvertent aneurysm rupture or blood vessel wall damage. In addition, what has been needed are methods and devices suitable for blocking blood flow in cerebral aneurysms over an extended period of time without a significant risk of deformation, compaction or dislocation.

Intrasaccular occlusive devices are part of a newer type of occlusion device used to treat various intravascular conditions including aneurysms. They are often more effective at treating these wide neck conditions, or larger treatment areas. The intrasaccular devices comprise a structure which sits within the aneurysm and provides an occlusive effect at the neck of the aneurysm to help limit blood flow into the aneurysm. The rest of the device comprises a relatively conformable structure that sits within the aneurysm helping to occlude all or a portion of the aneurysm. Intrasaccular devices typically conform to the shape of the treatment site. These devices also occlude the cross section of the neck of the treatment site/aneurysm, thereby promoting clotting and causing thrombosis and closing of the aneurysm over time. In larger aneurysms, there is a risk of compaction where the intrasaccular device can migrate into the aneurysm and leave the neck region.

Many intrasaccular devices are best suited to treat bifurcation aneurysms (aneurysms located along a vessel bifurcation) rather than sidewall aneurysms (which are located along a sidewall of a vessel), for a few reasons. First, while access into a bifurcation aneurysm is relatively straightforward given that catheter access occurs directly along the parent artery that leads into the bifurcation aneurysm, this is more complicated in a sidewall aneurysm where the catheter has to be angled into the aneurysm. In practice, this means that it is likely that the intrasaccular device may be delivered at an offset angle into the sidewall aneurysm in a number of circumstances. Second, the proximal end of some intrasaccular devices may be stiff due to the presence of, e.g., the braided wires comprising the implant being bundled together at a proximal terminus. The stiffness of the connection of the intrasaccular device with the pusher of the delivery system can hamper delivery of the intrasaccular device into sidewall aneurysms. Delivery into sidewall aneurysms (e.g., at about a 90° angle to the parent artery—though this can vary depending on the geometry of the sidewall aneurysm) requires a flexible connection between the pusher and implant while maintaining the pushability, trackability, and retrievable properties of the intrasaccular device.

Though intrasaccular devices offer some advantages in occluding target areas such as aneurysms, due to the tight geometry associated with the vasculature, it can be difficult to ensure that part of the intrasaccular devices does not stick out into the parent artery. It can also be difficult to sufficiently occlude flow at the neck of the aneurysm/treatment site. Furthermore, it can be difficult to configure an intrasaccular device that can effectively treat sidewall aneurysms. There is a need for an intrasaccular device that mitigates or prevents these issues.

SUMMARY

Intrasaccular device delivery into a sidewall aneurysm can be difficult for several reasons, as outlined above. For instance, the delivery catheter has to often be delivered at an odd angle due to the geometry of the sidewall aneurysm, making it difficult to correctly deliver and deploy the intrasaccular device. Furthermore, the proximal end of some intrasaccular devices may be stiff due to the presence of, e.g., implant wires being bundled together. The stiffness of the connection of the intrasaccular device with the pusher of the delivery system can hamper delivery of the intrasaccular device into sidewall aneurysms. Delivery into sidewall aneurysms (e.g., at a 90° angle to the parent artery) requires a flexible connection between the pusher and implant while maintaining the pushability, trackability, and retrievable properties of the intrasaccular device. Devices are described herein that address these problems by including a flexible connection between the pusher and the implant.

Devices are also described that increase proximal stability of the device and promotes proper seating of the device in the treatment location.

Devices are also described that further improve metal surface coverage at the proximal end of the device, thereby preventing compaction of the device.

An intrasaccular occlusive device is described. In one embodiment, the intrasaccular occlusive device has a first occlusive section that occludes the target structure, and a second occlusive section attached to the first occlusive section. The second occlusive section is meant to sit at the neck of the target region, thereby occluding flow at the neck section while also conforming to the neck shape such that it sets at/within this neck shape. In one embodiment, the first and second occlusive sections comprise a mesh of braided wires. In one embodiment, the first occlusive section includes a proximal dimpled region, and the second occlusive section is configured to fit within this proximal dimpled region. In one embodiment, the first occlusive section includes a proximal dimpled region with a stem, and the second occlusive section connects to the stem of the proximal dimpled region.

The intrasaccular devices could be used to treat bifurcation aneurysms located at ICA terminus, AComm, and MCA bifurcations. Devices are also described that aid in the delivery of intrasaccular devices into sidewall aneurysms.

In one embodiment, a device for treatment of a patient's cerebral aneurysm is described. The device includes a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the expanded state of the second permeable shell is configured to sit within the recessed section of the first permeable shell. The proximal end of the first permeable shell is coupled with the distal end of the second permeable shell.

In another embodiment, a cerebral sidewall aneurysm treatment device is described. The device includes a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the distal end of the second permeable shell is coupled to the proximal end of the first permeable shell, and wherein the proximal end of the second permeable shell is coupled with a delivery pusher. The second permeable shell is configured to exert force against the recessed section of the first permeable shell in order to position the first permeable shell over a neck region of the cerebral sidewall aneurysm.

In another embodiment, a device for treatment of a patient's cerebral aneurysm is described. The device includes a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section adapted to sit over a neck of an aneurysm; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the distal end of the second permeable shell is coupled with the proximal end of the first permeable shell. The second permeable shell is configured to occupy the recessed section of the first permeable shell to augment surface coverage over the neck of the aneurysm.

In another embodiment, a method for treating a cerebral aneurysm having an interior cavity and a neck is described. The method includes the step of advancing an implant in a microcatheter to a region of interest in a cerebral artery. The implant comprises a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a lumen of the microcatheter, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a concave section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within the lumen of the microcatheter, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the expanded state of the second permeable shell is configured to sit within the concave section of the first permeable shell, wherein the distal end of the second permeable shell is coupled with the proximal end of the first permeable shell. The first permeable shell is then deployed within the cerebral aneurysm, wherein the first permeable shell expands to the expanded state in the interior cavity of the aneurysm. The second permeable shell is then deployed, wherein the second permeable shell expands to the expanded state and sits within the concave section of the first permeable shell. The microcatheter is then withdrawn from the region of interest after deploying the second permeable shell.

In another embodiment, a device for treatment of a patient's cerebral aneurysm is described. The device includes a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a concave section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the expanded state of the second permeable shell is configured to sit within the concave section of the first permeable shell. The proximal end of the first permeable shell is coupled with the distal end of the second permeable shell.

In another embodiment, methods for treating a cerebral aneurysm having an interior cavity and a neck are described. The methods include the step of advancing an implant in a microcatheter to a region of interest in a cerebral artery, wherein the implant comprises a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a lumen of the microcatheter, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a concave section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within the lumen of the microcatheter, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the expanded state of the second permeable shell is configured to sit within the concave section of the first permeable shell. The proximal end of the first permeable shell is coupled with the distal end of the second permeable shell. The first permeable shell is then deployed within the cerebral aneurysm, wherein the first permeable shell expands to the expanded state in the interior cavity of the aneurysm. The second permeable shell is then deployed, wherein the second permeable shell expands to the expanded state and sits within the concave section of the first permeable shell. The microcatheter is then withdrawn from the region of interest after deploying the second permeable shell.

In one embodiment, a device for treatment of a patient's cerebral aneurysm is described. The device includes a first permeable shell and a second permeable shell. The first permeable shell has a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh. The expanded state has a proximal end with a concave section. The second permeable shell has a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, a first expanded state, a second expanded state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the second expanded state of the second permeable shell is configured to sit within the concave section of the first permeable shell. The proximal end of the first permeable shell is coupled with the distal end of the second permeable shell.

In another embodiment, methods for treating a cerebral aneurysm having an interior cavity and a neck are described. The methods include the step of advancing an implant in a microcatheter to a region of interest in a cerebral artery, wherein the implant comprises a first permeable shell and a second permeable shell. The first permeable shell has a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh. The expanded state has a proximal end with a concave section. The second permeable shell has a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, a first expanded state, a second expanded state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the second expanded state of the second permeable shell is configured to sit within the concave section of the first permeable shell. The proximal end of the first permeable shell is coupled with the distal end of the second permeable shell. The first permeable shell is then deployed within the cerebral aneurysm, wherein the first permeable shell expands to the expanded state in the interior cavity of the aneurysm. The second permeable shell is then deployed, wherein the second permeable shell expands to the first expanded state. The microcatheter is then withdrawn from the region of interest after the second permeable shell assumes the second expanded state and sits within the concave section of the first permeable shell.

In some embodiments, the first and second permeable shells may be coupled together, wherein juncture of the coupling serves as a flexible joint around which the first permeable shell can pivot and deflect relative to the second permeable shell. The first and second permeable shells may be coupled together with an elongate braided mesh. The flexible joint between the first and second permeable shell allows for the first permeable shell to deflect at an angle of up to about 180°, alternatively up to about 150°, alternatively up to about 120°, alternatively up to about 90°, alternatively up to about 60°, alternatively up to about 45°, alternatively up to about 30°, alternatively up to about 10° relative to a longitudinal axis of the second permeable shell. In some embodiments, the deflection or articulation highlighted above can help position or stabilize an intrasaccular device for delivery into a sidewall aneurysm.

In some embodiments, the second permeable shell may have an expanded convex shape that is configured to mate with the proximal concave or recessed section of the expanded state of the first permeable shell. In some embodiments, the second permeable shell is fully contained within the proximal concave cavity of the first permeable shell, i.e., the second permeable shell does not extend proximally past a plane defined by the proximal most edge of the first permeable shell when both the first and second permeable shells are in their expanded states. In other embodiments, the second permeable shell may be even with the plane defined by the proximal most edge of the first permeable shell when both the first and second permeable shells are in their expanded states. In other embodiments, the second permeable shell may extend proximally beyond the plane defined by the proximal most edge of the first permeable shell when both the first and second permeable shells are in their expanded states.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an elevation view of an embodiment of a device for treatment of a patient's vasculature and a plurality of arrows indicating inward radial force.

FIG. 2 is an elevation view of a beam supported by two simple supports and a plurality of arrows indicating force against the beam.

FIG. 3 is a bottom perspective view of an embodiment of a device for treatment of a patient's vasculature.

FIG. 4 is an elevation view of the device for treatment of a patient's vasculature of FIG. 3.

FIG. 5 is a transverse cross sectional view of the device of FIG. 4 taken along lines 5-5 in FIG. 4.

FIG. 6 shows the device of FIG. 4 in longitudinal section taken along lines 6-6 in FIG. 4.

FIG. 7 is an enlarged view of the woven filament structure taken from the encircled portion 7 shown in FIG. 5.

FIG. 8 is an enlarged view of the woven filament structure taken from the encircled portion 8 shown in FIG. 6.

FIG. 9 is a proximal end view of the device of FIG. 3.

FIG. 10 is a transverse sectional view of a proximal hub portion of the device in FIG. 6 indicated by lines 10-10 in FIG. 6.

FIG. 11 is an elevation view in partial section of a distal end of a delivery catheter with the device for treatment of a patient's vasculature of FIG. 3 disposed therein in a collapsed constrained state.

FIG. 12 illustrates an embodiment of a filament configuration for a device for treatment of a patient's vasculature.

FIG. 13 illustrates a device for treatment of a patient's vasculature.

FIG. 14 illustrates a device for treatment of a patient's vasculature that includes multiple permeable shells.

FIG. 15 illustrates the device for treatment of a patient's vasculature from FIG. 14 with the second permeable shell in a first expanded state.

FIGS. 16A-16E illustrates the device of FIG. 15 being delivered into a sidewall aneurysm.

FIG. 17 is a schematic view of a patient being accessed by an introducer sheath, a microcatheter and a device for treatment of a patient's vasculature releasably secured to a distal end of a delivery device or actuator.

FIG. 18 is a sectional view of a terminal aneurysm.

FIG. 19 is a sectional view of an aneurysm.

FIG. 20 is a schematic view in section of an aneurysm showing perpendicular arrows which indicate interior nominal longitudinal and transverse dimensions of the aneurysm.

FIG. 21 is a schematic view in section of the aneurysm of FIG. 20 with a dashed outline of a device for treatment of a patient's vasculature in a relaxed unconstrained state that extends transversely outside of the walls of the aneurysm.

FIG. 22 is a schematic view in section of an outline of a device represented by the dashed line in FIG. 21 in a deployed and partially constrained state within the aneurysm.

FIGS. 23-26 show a deployment sequence of a device for treatment of a patient's vasculature.

FIG. 27 is an elevation view in partial section of an embodiment of a device for treatment of a patient's vasculature deployed within an aneurysm at a tilted angle.

FIG. 28 is an elevation view in partial section of an embodiment of a device for treatment of a patient's vasculature deployed within an irregularly shaped aneurysm.

FIG. 29 shows an elevation view in section of a device for treatment of a patient's vasculature deployed within a vascular defect aneurysm.

DETAILED DESCRIPTION

Discussed herein are devices and methods for the treatment of vascular defects that are suitable for minimally invasive deployment within a patient's vasculature, and particularly, within the cerebral vasculature of a patient. For such embodiments to be safely and effectively delivered to a desired treatment site and effectively deployed, some device embodiments may be configured for collapse to a low profile constrained state with a transverse dimension suitable for delivery through an inner lumen of a microcatheter and deployment from a distal end thereof. Embodiments of these devices may also maintain a clinically effective configuration with sufficient mechanical integrity once deployed so as to withstand dynamic forces within a patient's vasculature over time that may otherwise result in compaction of a deployed device. It may also be desirable for some device embodiments to acutely occlude a vascular defect of a patient during the course of a procedure in order to provide more immediate feedback regarding success of the treatment to a treating physician.

Intrasaccular occlusive devices that include a permeable shell formed from a woven or braided mesh have been described in US 2017/0095254, US 2016/0249934, US 2016/0367260, US 2016/0249937, and US 2018/0000489, all of which are hereby expressly incorporated by reference in their entirety for all purposes.

Some embodiments are particularly useful for the treatment of cerebral aneurysms by reconstructing a vascular wall so as to wholly or partially isolate a vascular defect from a patient's blood flow. Some embodiments may be configured to be deployed within a vascular defect to facilitate reconstruction, bridging of a vessel wall or both in order to treat the vascular defect. For some of these embodiments, the permeable shell of the device may be configured to anchor or fix the permeable shell in a clinically beneficial position. For some embodiments, the device may be disposed in whole or in part within the vascular defect in order to anchor or fix the device with respect to the vascular structure or defect. The permeable shell may be configured to span an opening, neck or other portion of a vascular defect in order to isolate the vascular defect, or a portion thereof, from the patient's nominal vascular system in order allow the defect to heal or to otherwise minimize the risk of the defect to the patient's health.

For some or all of the embodiments of devices for treatment of a patient's vasculature discussed herein, the permeable shell may be configured to allow some initial perfusion of blood through the permeable shell. The porosity of the permeable shell may be configured to sufficiently isolate the vascular defect so as to promote healing and isolation of the defect, but allow sufficient initial flow through the permeable shell so as to reduce or otherwise minimize the mechanical force exerted on the membrane the dynamic flow of blood or other fluids within the vasculature against the device. For some embodiments of devices for treatment of a patient's vasculature, only a portion of the permeable shell that spans the opening or neck of the vascular defect, sometimes referred to as a defect spanning portion, need be permeable and/or conducive to thrombus formation in a patient's bloodstream. For such embodiments, that portion of the device that does not span an opening or neck of the vascular defect may be substantially non-permeable or completely permeable with a pore or opening configuration that is too large to effectively promote thrombus formation.

In general, it may be desirable in some cases to use a hollow, thin walled device with a permeable shell of resilient material that may be constrained to a low profile for delivery within a patient. Such a device may also be configured to expand radially outward upon removal of the constraint such that the shell of the device assumes a larger volume and fills or otherwise occludes a vascular defect within which it is deployed. The outward radial expansion of the shell may serve to engage some or all of an inner surface of the vascular defect whereby mechanical friction between an outer surface of the permeable shell of the device and the inside surface of the vascular defect effectively anchors the device within the vascular defect. Some embodiments of such a device may also be partially or wholly mechanically captured within a cavity of a vascular defect, particularly where the defect has a narrow neck portion with a larger interior volume. In order to achieve a low profile and volume for delivery and be capable of a high ratio of expansion by volume, some device embodiments include a matrix of woven or braided filaments that are coupled together by the interwoven structure so as to form a self-expanding permeable shell having a pore or opening pattern between couplings or intersections of the filaments that is substantially regularly spaced and stable, while still allowing for conformity and volumetric constraint.

As used herein, the terms woven and braided are used interchangeably to mean any form of interlacing of filaments to form a mesh structure. In the textile and other industries, these terms may have different or more specific meanings depending on the product or application such as whether an article is made in a sheet or cylindrical form. For purposes of the present disclosure, these terms are used interchangeably.

For some embodiments, three factors may be critical for a woven or braided wire occlusion device for treatment of a patient's vasculature that can achieve a desired clinical outcome in the endovascular treatment of cerebral aneurysms. We have found that for effective use in some applications, it may be desirable for the implant device to have sufficient radial stiffness for stability, limited pore size for near-complete acute (intra-procedural) occlusion and a collapsed profile which is small enough to allow insertion through an inner lumen of a microcatheter. A device with a radial stiffness below a certain threshold may be unstable and may be at higher risk of embolization in some cases. Larger pores between filament intersections in a braided or woven structure may not generate thrombus and occlude a vascular defect in an acute setting and thus may not give a treating physician or health professional such clinical feedback that the flow disruption will lead to a complete and lasting occlusion of the vascular defect being treated. Delivery of a device for treatment of a patient's vasculature through a standard microcatheter may be highly desirable to allow access through the tortuous cerebral vasculature in the manner that a treating physician is accustomed. A detailed discussion of radial stiffness, pore size, and the necessary collapsed profile can be found in US 2017/0095254, which was previously expressly incorporated by reference in its entirety.

As has been discussed, some embodiments of devices for treatment of a patient's vasculature call for sizing the device which approximates (or with some over-sizing) the vascular site dimensions to fill the vascular site. One might assume that scaling of a device to larger dimensions and using larger filaments would suffice for such larger embodiments of a device. However, for the treatment of brain aneurysms, the diameter or profile of the radially collapsed device is limited by the catheter sizes that can be effectively navigated within the small, tortuous vessels of the brain. Further, as a device is made larger with a given or fixed number of resilient filaments having a given size or thickness, the pores or openings between junctions of the filaments are correspondingly larger. In addition, for a given filament size the flexural modulus or stiffness of the filaments and thus the structure decrease with increasing device dimension. Flexural modulus may be defined as the ratio of stress to strain. Thus, a device may be considered to have a high flexural modulus or be stiff if the strain (deflection) is low under a given force. A stiff device may also be said to have low compliance.

To properly configure larger size devices for treatment of a patient's vasculature, it may be useful to model the force on a device when the device is deployed into a vascular site or defect, such as a blood vessel or aneurysm, that has a diameter or transverse dimension that is smaller than a nominal diameter or transverse dimension of the device in a relaxed unconstrained state. As discussed, it may be advisable to “over-size” the device in some cases so that there is a residual force between an outside surface of the device and an inside surface of the vascular wall. The inward radial force on a device 10 that results from over-sizing is illustrated schematically in FIG. 1 with the arrows 12 in the figure representing the inward radial force. As shown in FIG. 2, these compressive forces on the filaments 14 of the device in FIG. 1 can be modeled as a simply supported beam 16 with a distributed load or force as show by the arrows 18 in the figure. It can be seen from the equation below for the deflection of a beam with two simple supports 20 and a distributed load that the deflection is a function of the length, L to the 4^(th) power:

Deflection of Beam=5FL ⁴/384El

where

-   -   F=force,     -   L=length of beam,     -   E=Young's Modulus, and     -   l=moment of inertia.

Thus, as the size of the device increases and L increases, the compliance increases substantially. Accordingly, an outward radial force exerted by an outside surface of the filaments 14 of the device 10 against a constraining force when inserted into a vascular site such as blood vessel or aneurysm is lower for a given amount of device compression or over-sizing. This force may be important in some applications to assure device stability and to reduce the risk of migration of the device and potential distal embolization.

In some embodiments, a combination of small and large filament sizes may be utilized to make a device with a desired radial compliance and yet have a collapsed profile which is configured to fit through an inner lumen of commonly used microcatheters. A device fabricated with even a small number of relatively large filaments 14 can provide reduced radial compliance (or increased stiffness) compared to a device made with all small filaments. Even a relatively small number of larger filaments may provide a substantial increase in bending stiffness due to change in the moment of Inertia that results from an increase in diameter without increasing the total cross sectional area of the filaments. The moment of inertia (I) of a round wire or filament may be defined by the equation:

I=πd ⁴/64

-   -   where d is the diameter of the wire or filament.

Since the moment of inertia is a function of filament diameter to the fourth power, a small change in the diameter greatly increases the moment of inertia. Thus, small changes in filament size can have substantial impact on the deflection at a given load and thus the compliance of the device.

Thus, the stiffness can be increased by a significant amount without a large increase in the cross sectional area of a collapsed profile of the device 10. This may be particularly important as device embodiments are made larger to treat large aneurysms. While large cerebral aneurysms may be relatively rare, they present an important therapeutic challenge as some embolic devices currently available to physicians have relatively poor results compared to smaller aneurysms.

As such, some embodiments of devices for treatment of a patient's vasculature may be formed using a combination of filaments 14 with a number of different diameters such as 2, 3, 4, 5 or more different diameters or transverse dimensions. In device embodiments where filaments with two different diameters are used, some larger filament embodiments may have a transverse dimension of about 0.001 inches to about 0.004 inches and some small filament embodiments may have a transverse dimension or diameter of about 0.0004 inches and about 0.0015 inches, more specifically, about 0.0004 inches to about 0.001 inches. The ratio of the number of large filaments to the number of small filaments may be between about 2 and 12 and may also be between about 4 and 8. In some embodiments, the difference in diameter or transverse dimension between the larger and smaller filaments may be less than about 0.004 inches, more specifically, less than about 0.0035 inches, and even more specifically, less than about 0.002 inches.

As discussed above, device embodiments 10 for treatment of a patient's vasculature may include a plurality of wires, fibers, threads, tubes or other filamentary elements that form a structure that serves as a permeable shell. For some embodiments, a globular shape may be formed from such filaments by connecting or securing the ends of a tubular braided structure. For such embodiments, the density of a braided or woven structure may inherently increase at or near the ends where the wires or filaments 14 are brought together and decrease at or near a middle portion 30 disposed between a proximal end 32 and distal end 34 of the permeable shell 40. For some embodiments, an end or any other suitable portion of a permeable shell 40 may be positioned in an opening or neck of a vascular defect such as an aneurysm for treatment. As such, a braided or woven filamentary device with a permeable shell may not require the addition of a separate defect spanning structure having properties different from that of a nominal portion of the permeable shell to achieve hemostasis and occlusion of the vascular defect. Such a filamentary device may be fabricated by braiding, weaving or other suitable filament fabrication techniques. Such device embodiments may be shape set into a variety of three-dimensional shapes such as discussed herein.

Referring to FIGS. 3-10, an embodiment of a device for treatment of a patient's vasculature 10 is shown. The device 10 includes a self-expanding resilient permeable shell 40 having a proximal end 32, a distal end 34, a longitudinal axis 46 and further comprising a plurality of elongate resilient filaments 14 including large filaments 48 and small filaments 50 of at least two different transverse dimensions as shown in more detail in FIGS. 5, 7, and 8. The filaments 14 have a woven structure and are secured relative to each other at proximal ends 60 and distal ends 62 thereof. The permeable shell 40 of the device has a radially constrained elongated state configured for delivery within a microcatheter 61, as shown in FIG. 11, with the thin woven filaments 14 extending longitudinally from the proximal end 42 to the distal end 44 radially adjacent each other along a length of the filaments.

As shown in FIGS. 3-6, the permeable shell 40 also has an expanded relaxed state with a globular and longitudinally shortened configuration relative to the radially constrained state. In the expanded state, the woven filaments 14 form the self-expanding resilient permeable shell 40 in a smooth path radially expanded from a longitudinal axis 46 of the device between the proximal end 32 and distal end 34. The woven structure of the filaments 14 includes a plurality of openings 64 in the permeable shell 40 formed between the woven filaments. For some embodiments, the largest of said openings 64 may be configured to allow blood flow through the openings only at a velocity below a thrombotic threshold velocity. Thrombotic threshold velocity has been defined, at least by some, as the time-average velocity at which more than 50% of a vascular graft surface is covered by thrombus when deployed within a patient's vasculature. In the context of aneurysm occlusion, a slightly different threshold may be appropriate. Accordingly, the thrombotic threshold velocity as used herein shall include the velocity at which clotting occurs within or on a device, such as device 10, deployed within a patient's vasculature such that blood flow into a vascular defect treated by the device is substantially blocked in less than about 1 hour or otherwise during the treatment procedure. The blockage of blood flow into the vascular defect may be indicated in some cases by minimal contrast agent entering the vascular defect after a sufficient amount of contrast agent has been injected into the patient's vasculature upstream of the implant site and visualized as it dissipates from that site. Such sustained blockage of flow within less than about 1 hour or during the duration of the implantation procedure may also be referred to as acute occlusion of the vascular defect.

As such, once the device 10 is deployed, any blood flowing through the permeable shell may be slowed to a velocity below the thrombotic threshold velocity and thrombus will begin to form on and around the openings in the permeable shell 40. Ultimately, this process may be configured to produce acute occlusion of the vascular defect within which the device 10 is deployed. For some embodiments, at least the distal end of the permeable shell 40 may have a reverse bend in an everted configuration such that the secured distal ends 62 of the filaments 14 are withdrawn axially within the nominal permeable shell structure or contour in the expanded state. For some embodiments, the proximal end of the permeable shell further includes a reverse bend in an everted configuration such that the secured proximal ends 60 of the filaments 14 are withdrawn axially within the nominal permeable shell structure 40 in the expanded state. As used herein, the term everted may include a structure that is everted, partially everted and/or recessed with a reverse bend as shown in the device embodiment of FIGS. 3-6. For such embodiments, the ends 60 and 62 of the filaments 14 of the permeable shell or hub structure disposed around the ends may be withdrawn within or below the globular shaped periphery of the permeable shell of the device.

The elongate resilient filaments 14 of the permeable shell 40 may be secured relative to each other at proximal ends 60 and distal ends 62 thereof by one or more methods including welding, soldering, adhesive bonding, epoxy bonding or the like. In addition to the ends of the filaments being secured together, a distal hub 66 may also be secured to the distal ends 62 of the thin filaments 14 of the permeable shell 40 and a proximal hub 68 secured to the proximal ends 60 of the thin filaments 14 of the permeable shell 40. The proximal hub 68 may include a cylindrical member that extends proximally beyond the proximal ends 60 of the thin filaments so as to form a cavity 70 within a proximal portion of the proximal hub 68. The proximal cavity 70 may be used for holding adhesives such as epoxy, solder or any other suitable bonding agent for securing an elongate detachment tether 72 that may in turn be detachably secured to a delivery apparatus such as is shown in FIG. 11.

For some embodiments, the elongate resilient filaments 14 of the permeable shell 40 may have a transverse cross section that is substantially round in shape and be made from a superelastic material that may also be a shape memory metal. The shape memory metal of the filaments of the permeable shell 40 may be heat set in the globular configuration of the relaxed expanded state as shown in FIGS. 3-6. Suitable superelastic shape memory metals may include alloys such as NiTi alloy and the like. The superelastic properties of such alloys may be useful in providing the resilient properties to the elongate filaments 14 so that they can be heat set in the globular form shown, fully constrained for delivery within an inner lumen of a microcatheter and then released to self expand back to substantially the original heat set shape of the globular configuration upon deployment within a patient's body.

The device 10 may have an everted filamentary structure with a permeable shell 40 having a proximal end 32 and a distal end 34 in an expanded relaxed state. The permeable shell 40 has a substantially enclosed configuration for the embodiments shown. Some or all of the permeable shell 40 of the device 10 may be configured to substantially block or impede fluid flow or pressure into a vascular defect or otherwise isolate the vascular defect over some period of time after the device is deployed in an expanded state. The permeable shell 40 and device 10 generally also has a low profile, radially constrained state, as shown in FIG. 11, with an elongated tubular or cylindrical configuration that includes the proximal end 32, the distal end 34 and a longitudinal axis 46. While in the radially constrained state, the elongate flexible filaments 14 of the permeable shell 40 may be disposed substantially parallel and in close lateral proximity to each other between the proximal end and distal end forming a substantially tubular or compressed cylindrical configuration.

Proximal ends 60 of at least some of the filaments 14 of the permeable shell 40 may be secured to the proximal hub 68 and distal ends 62 of at least some of the filaments 14 of the permeable shell 40 are secured to the distal hub 66, with the proximal hub 68 and distal hub 66 being disposed substantially concentric to the longitudinal axis 46 as shown in FIG. 4. The ends of the filaments 14 may be secured to the respective hubs 66 and 68 by any of the methods discussed above with respect to securement of the filament ends to each other, including the use of adhesives, solder, welding and the like. A middle portion 30 of the permeable shell 40 may have a first transverse dimension with a low profile suitable for delivery from a microcatheter as shown in FIG. 11. Radial constraint on the device 10 may be applied by an inside surface of the inner lumen of a microcatheter, such as the distal end portion of the microcatheter 61 shown, or it may be applied by any other suitable mechanism that may be released in a controllable manner upon ejection of the device 10 from the distal end of the catheter. In FIG. 11 a proximal end or hub 68 of the device 10 is secured to a distal end of an elongate delivery apparatus 111 of a delivery system 112 disposed at the proximal hub 68 of the device 10. Additional details of delivery devices can be found in, e.g., US 2016/0367260, which was previously incorporated by reference in its entirety.

Some device embodiments 10 having a braided or woven filamentary structure may be formed using about 10 filaments to about 300 filaments 14, more specifically, about 10 filaments to about 100 filaments 14, and even more specifically, about 60 filaments to about 80 filaments 14. Some embodiments of a permeable shell 40 may include about 70 filaments to about 300 filaments extending from the proximal end 32 to the distal end 34, more specifically, about 100 filaments to about 200 filaments extending from the proximal end 32 to the distal end 34. For some embodiments, the filaments 14 may have a transverse dimension or diameter of about 0.0008 inches to about 0.004 inches. The elongate resilient filaments 14 in some cases may have an outer transverse dimension or diameter of about 0.0005 inch to about 0.005 inch, more specifically, about 0.001 inch to about 0.003 inch, and in some cases about 0.0004 inches to about 0.002 inches. For some device embodiments 10 that include filaments 14 of different sizes, the large filaments 48 of the permeable shell 40 may have a transverse dimension or diameter that is about 0.001 inches to about 0.004 inches and the small filaments 50 may have a transverse dimension or diameter of about 0.0004 inches to about 0.0015 inches, more specifically, about 0.0004 inches to about 0.001 inches. In addition, a difference in transverse dimension or diameter between the small filaments 50 and the large filaments 48 may be less than about 0.004 inches, more specifically, less than about 0.0035 inches, and even more specifically, less than about 0.002 inches. For embodiments of permeable shells 40 that include filaments 14 of different sizes, the number of small filaments 50 of the permeable shell 40 relative to the number of large filaments 48 of the permeable shell 40 may be about 2 to 1 to about 15 to 1, more specifically, about 2 to 1 to about 12 to 1, and even more specifically, about 4 to 1 to about 8 to 1.

The expanded relaxed state of the permeable shell 40, as shown in FIG. 4, has an axially shortened configuration relative to the constrained state such that the proximal hub 68 is disposed closer to the distal hub 66 than in the constrained state. Both hubs 66 and 68 are disposed substantially concentric to the longitudinal axis 46 of the device and each filamentary element 14 forms a smooth arc between the proximal and distal hubs 66 and 68 with a reverse bend at each end. A longitudinal spacing between the proximal and distal hubs 66 and 68 of the permeable shell 40 in a deployed relaxed state may be about 25 percent to about 75 percent of the longitudinal spacing between the proximal and distal hubs 66 and 68 in the constrained cylindrical state, for some embodiments. The arc of the filaments 14 between the proximal and distal ends 32 and 34 may be configured such that a middle portion of each filament 14 has a second transverse dimension substantially greater than the first transverse dimension.

For some embodiments, the permeable shell 40 may have a first transverse dimension in a collapsed radially constrained state of about 0.2 mm to about 2 mm and a second transverse dimension in a relaxed expanded state of about 4 mm to about 30 mm. For some embodiments, the second transverse dimension of the permeable shell 40 in an expanded state may be about 2 times to about 150 times the first transverse dimension, more specifically, about 10 times to about 25 times the first or constrained transverse dimension. A longitudinal spacing between the proximal end 32 and distal end 34 of the permeable shell 40 in the relaxed expanded state may be about 25% percent to about 75% percent of the spacing between the proximal end 32 and distal end 34 in the constrained cylindrical state. For some embodiments, a major transverse dimension of the permeable shell 40 in a relaxed expanded state may be about 4 mm to about 30 mm, more specifically, about 9 mm to about 15 mm, and even more specifically, about 4 mm to about 8 mm.

An arced portion of the filaments 14 of the permeable shell 40 may have a sinusoidal-like shape with a first or outer radius 88 and a second or inner radius 90 near the ends of the permeable shell 40 as shown in FIG. 6. This sinusoid-like or multiple curve shape may provide a concavity in the proximal end 32 that may reduce an obstruction of flow in a parent vessel adjacent a vascular defect. For some embodiments, the first radius 88 and second radius 90 of the permeable shell 40 may be between about 0.12 mm to about 3 mm. For some embodiments, the distance between the proximal end 32 and distal end 34 may be less than about 60% of the overall length of the permeable shell 40 for some embodiments. Such a configuration may allow for the distal end 34 to flex downward toward the proximal end 32 when the device 10 meets resistance at the distal end 34 and thus may provide longitudinal conformance. The filaments 14 may be shaped in some embodiments such that there are no portions that are without curvature over a distance of more than about 2 mm. Thus, for some embodiments, each filament 14 may have a substantially continuous curvature. This substantially continuous curvature may provide smooth deployment and may reduce the risk of vessel perforation. For some embodiments, one of the ends 32 or 34 may be retracted or everted to a greater extent than the other so as to be more longitudinally or axially conformal than the other end.

The first radius 88 and second radius 90 of the permeable shell 40 may be between about 0.12 mm to about 3 mm for some embodiments. For some embodiments, the distance between the proximal end 32 and distal end 34 may be more than about 60% of the overall length of the expanded permeable shell 40. Thus, the largest longitudinal distance between the inner surfaces may be about 60% to about 90% of the longitudinal length of the outer surfaces or the overall length of device 10. A gap between the hubs 66 and 68 at the proximal end 32 and distal end 34 may allow for the distal hub 66 to flex downward toward the proximal hub 68 when the device 10 meets resistance at the distal end and thus provides longitudinal conformance. The filaments 14 may be shaped such that there are no portions that are without curvature over a distance of more than about 2 mm. Thus, for some embodiments, each filament 14 may have a substantially continuous curvature. This substantially continuous curvature may provide smooth deployment and may reduce the risk of vessel perforation. The distal end 34 may be retracted or everted to a greater extent than the proximal end 32 such that the distal end portion of the permeable shell 40 may be more radially conformal than the proximal end portion. Conformability of a distal end portion may provide better device conformance to irregular shaped aneurysms or other vascular defects. A convex surface of the device may flex inward forming a concave surface to conform to curvature of a vascular site.

FIG. 10 shows an enlarged view of the filaments 14 disposed within a proximal hub 68 of the device 10 with the filaments 14 of two different sizes constrained and tightly packed by an outer ring of the proximal hub 68. The tether member 72 may optionally be disposed within a middle portion of the filaments 14 or within the cavity 70 of the proximal hub 68 proximal of the proximal ends 60 of the filaments 14 as shown in FIG. 6. The distal end of the tether 72 may be secured with a knot 92 formed in the distal end thereof which is mechanically captured in the cavity 70 of the proximal hub 68 formed by a proximal shoulder portion 94 of the proximal hub 68. The knotted distal end 92 of the tether 72 may also be secured by bonding or potting of the distal end of the tether 72 within the cavity 70 and optionally amongst the proximal ends 60 of the filaments 14 with mechanical compression, adhesive bonding, welding, soldering, brazing or the like. The tether embodiment 72 shown in FIG. 6 has a knotted distal end 92 potted in the cavity of the proximal hub 68 with an adhesive. Such a tether 72 may be a dissolvable, severable or releasable tether that may be part of a delivery apparatus 111 used to deploy the device 10 as shown in FIG. 11 and FIGS. 23-26. FIG. 10 also shows the large filaments 48 and small filaments 50 disposed within and constrained by the proximal hub 68 which may be configured to secure the large and small filaments 48 and 50 in place relative to each other within the outer ring of the proximal hub 68.

FIGS. 7 and 8 illustrate some configuration embodiments of braided filaments 14 of a permeable shell 40 of the device 10 for treatment of a patient's vasculature. The braid structure in each embodiment is shown with a circular shape 100 disposed within a pore 64 of a woven or braided structure with the circular shape 100 making contact with each adjacent filament segment. The pore opening size may be determined at least in part by the size of the filament elements 14 of the braid, the angle overlapping filaments make relative to each other and the picks per inch of the braid structure. For some embodiments, the cells or openings 64 may have an elongated substantially diamond shape as shown in FIG. 7, and the pores or openings 64 of the permeable shell 40 may have a substantially more square shape toward a middle portion 30 of the device 10, as shown in FIG. 8. The diamond shaped pores or openings 64 may have a length substantially greater than the width particularly near the hubs 66 and 68. In some embodiments, the ratio of diamond shaped pore or opening length to width may exceed a ratio of 3 to 1 for some cells. The diamond-shaped openings 64 may have lengths greater than the width thus having an aspect ratio, defined as Length/Width of greater than 1. The openings 64 near the hubs 66 and 68 may have substantially larger aspect ratios than those farther from the hubs as shown in FIG. 7. The aspect ratio of openings 64 adjacent the hubs may be greater than about 4 to 1. The aspect ratio of openings 64 near the largest diameter may be between about 0.75 to 1 and about 2 to 1 for some embodiments. For some embodiments, the aspect ratio of the openings 64 in the permeable shell 40 may be about 0.5 to 1 to about 2 to 1.

The pore size defined by the largest circular shapes 100 that may be disposed within openings 64 of the braided structure of the permeable shell 40 without displacing or distorting the filaments 14 surrounding the opening 64 may range in size from about 0.005 inches to about 0.01 inches, more specifically, about 0.006 inches to about 0.009 inches, even more specifically, about 0.007 inches to about 0.008 inches for some embodiments. In addition, at least some of the openings 64 formed between adjacent filaments 14 of the permeable shell 40 of the device 10 may be configured to allow blood flow through the openings 64 only at a velocity below a thrombotic threshold velocity. For some embodiments, the largest openings 64 in the permeable shell structure 40 may be configured to allow blood flow through the openings 64 only at a velocity below a thrombotic threshold velocity. As discussed above, the pore size may be less than about 0.016 inches, more specifically, less than about 0.012 inches for some embodiments. For some embodiments, the openings 64 formed between adjacent filaments 14 may be about 0.005 inches to about 0.04 inches.

FIG. 12 illustrates in transverse cross section an embodiment of a proximal hub 68 showing the configuration of filaments which may be tightly packed and radially constrained by an inside surface of the proximal hub 68. In some embodiments, the braided or woven structure of the permeable shell 40 formed from such filaments 14 may be constructed using a large number of small filaments. The number of filaments 14 may be greater than 125 and may also be between about 80 filaments and about 180 filaments. As discussed above, the total number of filaments 14 for some embodiments may be about 70 filaments to about 300 filaments, more specifically, about 100 filaments to about 200 filaments. In some embodiments, the braided structure of the permeable shell 40 may be constructed with two or more sizes of filaments 14. For example, the structure may have several larger filaments that provide structural support and several smaller filaments that provide the desired pore size and density and thus flow resistance to achieve a thrombotic threshold velocity in some cases. For some embodiments, small filaments 50 of the permeable shell 40 may have a transverse dimension or diameter of about 0.0006 inches to about 0.002 inches for some embodiments and about 0.0004 inches to about 0.001 inches in other embodiments. The large filaments 48 may have a transverse dimension or diameter of about 0.0015 inches to about 0.004 inches in some embodiments and about 0.001 inches to about 0.004 inches in other embodiments. The filaments 14 may be braided in a plain weave that is one under, one over structure (shown in FIGS. 7 and 8) or a supplementary weave; more than one warp interlace with one or more than one weft. The pick count may be varied between about 25 and 200 picks per inch (PPI).

Intrasaccular occlusive devices, such as the one shown in FIG. 13, can sometimes utilize an apple-core braid winding shape, where a proximal 137 a and/or distal stem 137 b are include at or near the proximal 132 and distal 134 ends of device 110. The proximal stem 137 a represents the attachment junction with a mechanical pusher device used to place the device 110.

In some embodiments, a hub (sometimes configured as a tubular marker band) is used within this region as an attachment junction for all the associated wires comprising the device—meaning the various wires comprising the intrasaccular device may proximally terminate at the hub interface, as shown and described with respect to earlier embodiments (e.g., FIG. 6). One advantage of a tubular marker band (e.g. made of a radiopaque material such as tantalum, gold, platinum, or palladium) is enhanced visualization of the ends of the device when radiographic imaging is used. The wires can terminate/mate to an external surface of the hub, or along an internal lumen of the hub. The tubular marker band may sit over a terminal portion of the stem 137 a or 137 b. In some embodiments, as shown, (e.g., in FIG. 6) the hub/tubular marker does not extend proximally or distally beyond the length of the device itself. In other embodiments, the hub/tubular marker does extend proximally and/or distally beyond the length of the device such that it juts out proximally and/or distally beyond the rest of the mesh occlusive device—meaning the hub/tubular marker may extend proximally past a plane defined by the proximal most edge of the expanded state of the permeable shell 140, and distally beyond a plane defined by the distal most edge of the expanded state of the permeable shell 140.

The proximal stem 137 a can sit within a proximal dimpled, recessed, or concave section 133. Often this proximal dimpled, recessed, or concave section 133 helps ensure the device 110 can sit within the target region while also occluding the target region. In some circumstances, the proximal stem 137 a may jut out of the treatment site (e.g., aneurysm) and into the parent vessel when implanted due to various reasons. Some reasons may include the dimensions of the associated treatment site in which the device is occluding (e.g., the sizing of the device relative to the aneurysm), and/or the proximal neck opening of the aneurysm.

Generally, with intrasaccular occlusion devices or intrasaccular flow disruption devices, it is desirable to have a significant flow-disruption effect at the proximal end of the device to reduce the blood flow at the neck region—in turn, thereby reducing blood flow in the aneurysm. The mesh of braided wires forming the proximal dimpled region 133 of the device (the portion typically overlying the neck of the aneurysm) helps provide this flow-disruption effect. Intra-aneurysmal flow stagnation resulting from the flow disruption effect promotes thrombosis within the aneurysm and subsequent obliteration of the aneurysm over time.

Embodiments of this device augment flow-disruption at the proximal end of the device by providing an additional layer or permeable shell that can fill the proximal dimple, recessed, or concave section 133 located at a proximal region of the intrasaccular device. In some cases, these embodiments can facilitate easier placement of an intrasaccular device within a sidewall aneurysm.

An intrasaccular occlusive device 210 is shown in FIGS. 14-15. The device 210 includes an intrasaccular device portion 240 having a proximal recess 133 and a distal recess 135, similar to the embodiments described above. Furthermore, distal stem 137 b and proximal stem 237 a are utilized in each proximal recess 133 and distal recess 135 region. Distal stem 137 b is configured similar to the other embodiments, where a tubular hub or marker band (not shown) can be used along the distal end of the stem (e.g., as a distal terminus for the braided implant wires). A proximal stem 237 a is also used. In one embodiment, as shown in FIGS. 14-15, the proximal stem 237 a is shorter than the proximal stem 137 a of FIG. 13 and sits completely within the proximal dimpled or concave section 133. The proximal stem 237 a is connected to a second occlusive element 222.

Going further into the details of the intrasaccular device 210, device 210 includes two interconnected braided structures 240 and 222, which combine to form a barrel-like or globular-like structure. The overall occlusive device 210 will comprise the first (distally-oriented) occlusive element 240 and the second (proximally-oriented) occlusive element 222.

FIG. 15 shows a deployment configuration, whereby occlusive element 222 is in an elongated configuration. A proximal end of the occlusive element 222 is connected to a delivery pusher 243 (e.g., through a tubular hub or marker band 252 a), whereby the delivery pusher 243 is used to navigate device 210 (which includes intrasaccular portion 240 and second occlusive portion 222).

In a first delivery configuration, the occlusive element 222 adopts the elongated configuration shown in FIG. 15. In a delivered configuration, shown in FIG. 14, the occlusive element 222 adopts a radially expansile and longitudinally compressed configuration—whereby occlusive element 222 sits flush within the proximal dimple, recessed, or concave section 133 of the device 210 in a fully deployed configuration, thereby sealing the neck of the aneurysm/treatment site. The inclusion of the occlusive element 222, which can span the proximal recessed section 133 of device 210, augments the flow disruption effect at the proximal end (which spans the neck region of the aneurysm) of the device 210, due to the additional barrier to blood entry provided by this portion 222. By way of example, blood flowing into the neck region of the aneurysm would have to first pass by the wires of the occlusive portion 222, then the wires of the intrasaccular device portion 240. In this way, there is increased resistance to blood flow along the proximal, or neck-facing region of the device 210—thereby augmenting flow disruption at the proximal end of the device.

In one embodiment, both occlusive elements 240, 222 are created from wires made from a shape-memory alloy, such as nitinol wires and/or DFT (drawn filled tubes) and heat set into the shapes shown in FIG. 14. In one example, where DFT is used, the DFT is composed of a radiopaque (e.g., tantalum, platinum, gold, or palladium) core surrounded by a nitinol jacket. In one embodiment, only nitinol wires are used for occlusive elements 240, 222. In another embodiment, only DFT wires are used for occlusive elements 240, 222. In another embodiment, a mixture of nitinol and DFT wires are used along one or both of occlusive elements 240, 222 (e.g., where one is solely composed of nitinol and the other solely composed of DFT, or where one or both are composed of a mixture of DFT and nitinol wires).

In one example, the first occlusive element 240 is manufactured and heat set into the barrel-like structure having proximal 133 and distal 135 dimpled concave sections. The second occlusive element 222 is then manufactured and heat set such that the distally-facing (or upward facing, in the context of FIGS. 14-15) outer surface of the second occlusive element 222 is configured to conform or mate with the proximally-facing (or downward facing, in the context of the same figures) surface of the proximal dimpled region 133. The second occlusive element 222 is configured to adopt a convex shape that mates with the concave shape of the proximal dimpled section 133 when implanted. The two occlusive elements 240, 222 may be connected, for instance by a hub or marker band element. In alternative configurations, the first and second occlusive elements 240, 222 are made from the same tubular mesh (same woven filaments), where the second occlusive element is formed of wires which are tracked through the narrow diameter proximal stem region and then wound into the dimpled region of the first occlusive element. The device can be manufactured by wrapping a single tubular mesh around a fixture containing the shape of occlusive elements 240, 222. The fixture and the braided mesh can then be heat set to obtain the secondary shape memory. Thus, the first and second occlusive elements can either be completely separate mesh braids or can be formed from the same mesh braid wound in a particular configuration. Proximal hub or marker band 252 a (and a distal hub or marker band, not shown) can then be attached to the device, respectively, at the proximal and distal ends. The proximal hub or marker band 252 a can then be attached to a pusher 243.

In some configurations, a hub or marker band can be placed between occlusive element 222 and occlusive element 240. Where both elements are composed of the same wires, the wires are passed through a hub or marker band and then continue into the second occlusive element. Alternatively, where both elements are composed of the same wires, no hub or marker band is used and, instead, the wires simply extend from a distal end or region of occlusive portion 240, through stem 237 a, to the proximal end or region of occlusive portion 222. A device in which there is no hub or marker band between the first and second occlusive elements 240, 222 may be less stiff than an embodiment including a hub or marker band.

Where occlusive elements 240 and 222 are composed of different/separate wire braids, then a hub or marker band can be used between these two sections (e.g., along proximal stem 237 a) where the wires of occlusive element 240 terminate along an external or internal surface of the hub or marker band, and the separate wires of occlusive element 222 then begin along an external or internal surface of the same hub or marker band. Alternatively, the wires of occlusive element 240 proximally terminate at a first hub or marker band and the separate wires of occlusive element 222 begin at an adjacent hub or hub or marker band.

The second occlusive element 222, which bridges the space in the proximal dimpled or concave section 133 of the first occlusive element 240, has good shape retention properties that enable it to fit into the dimpled recessed shape of proximal dimpled region 133. Along with the provided occlusive benefit at the neck of the treatment site/aneurysm, the second occlusive element 222 also provides additional push strength as a bridge between the proximal mechanical pusher 243 and the distal first occlusive element, thereby providing more control during deployment.

FIG. 15 illustrates a configuration of the device when it is being delivered. The first occlusive element 240 adopts its heat seat, expanded configuration when freed from a delivery catheter (not shown). The proximal end of the first occlusive element 240 is connected to a distal end of the second occlusive element 222 through proximal stem or elongate proximal extension 237 a, which acts as a flexible joint allowing the first occlusive element 240 to pivot or flex relative to the second occlusive element 222. Upon delivery, the user distally advances the pusher 243 so that the proximal occlusive element 222 is pushed into recess 133 to occupy the space of the recess—such that the configuration in FIG. 14 is adopted. The pusher is then detached from the device 210 so that the device 210 remains as an implant.

As seen in FIGS. 16A-16E, the device 210 contains a braided region that acts as a flexible joint 237 a between the first 240 and second 222 occlusive elements. The device 210 is delivered using a microcatheter 61 and pusher 243, which is connected to a proximal end of the device 210. When delivery is attempted to an aneurysm, e.g., a sidewall aneurysm, the flexible joint between the first 240 and second 222 occlusive elements allows for easier delivery because the first occlusive element 240 is capable of deflecting or pivoting relative to a longitudinal axis formed by the pusher and the second permeable shell or a longitudinal axis of the second permeable shell. The flexible joint 237 a between the first and second occlusive elements allows for the first occlusive element 240 to deflect, bend, or flex at an angle of up to about 180°, alternatively up to about 150°, alternatively up to about 120°, alternatively up to about 90°, alternatively up to about 60°, alternatively up to about 45°, alternatively up to about 30°, alternatively up to about 10°. The second occlusive element 222 will generally adopt a more elongated shape during delivery, e.g., while in the microcatheter. After release from the lumen of the microcatheter but before placement within the proximal concave section of the first occlusive element 240, the second occlusive element 222 will adopt a first expanded state while the second occlusive element is under tension from a proximal direction. The first expanded state has a longer length and smaller radius than the second expanded state that the second occlusive element adopts after the proximal tension is released or a force is applied to push it against the proximal end of the first permeable shell. Upon placement within the aneurysm and release of the proximal tension, the second occlusive element 222 will abut the first occlusive element 240 within the proximal dimpled concave region 133 and assume the second expanded state, which is configured to sit within the proximal dimpled concave region 133. The deployment of device 210 with the second occlusive element 222 seated in the proximal dimpled concave region 133 assists in occluding blood flow at the proximal end of the device 210 and forming a strong proximal occlusive barrier to blood flow. The second occlusive element 222 will be heat set into a convex shape that generally fills the proximal concave section. Thus, it will readily adopt this convex shape that mates with the dimpled concave shape of the proximal region of the first occlusive device 210. The user will then detach the pusher 243 from the proximal end of the second occlusive element 222, thereby leaving the occlusive implant 210 within the target treatment region (e.g., an aneurysm 160).

The second occlusive device 222, along with providing increased resistance to blood flow at the neck of the aneurysm by filling in the recess 133, can also help pivot the connected occlusive portion 240 into a proper orientation after deployment into the treatment site. As discussed above, intrasaccular devices can be optimal treatments for bifurcation aneurysms where a catheter can be delivered directly from a parent artery into the aneurysm at a vessel bifurcation junction. This is more complicated for sidewall aneurysms, where the catheter often comes into the aneurysm at an odd, non-linear angle. As such, the intrasaccular device may be deployed at an odd angle, and closer to one side of the aneurysm rather than directly in the middle. This odd delivery angle can negatively affect flow disruption at the neck of the aneurysm, which can contribute to the intrasaccular device shifting within the aneurysm over time. Sidewall aneurysms also can be irregularly shaped, further making proper entry and seating of the intrasaccular device in the aneurysm difficult. Because the second occlusive device 222 is proximally oriented with respect to the primary occlusive portion 240, during implantation, the second occlusive portion 222 will exert force against the distally connected occlusive portion 240. This force or exertion can help orient the primary occlusive portion 240 into a proper orientation and position in the aneurysm after it is deployed from the delivery catheter. Depending on the angle and shape of the sidewall aneurysm, the sidewall aneurysm can be angled, for instance at about 90 degrees or between about 60-120 degrees relative to the parent artery. The secondary occlusive section 222 can help in articulating or positioning the overall intrasaccular device to be located in a proper orientation within the aneurysm. This is due to the force provided by the proximal occlusive portion 222, as well as the flexible nature of joint/stem 237 a, as described earlier.

Though the inclusion of the second or proximal occlusive section 222 offers some advantages in deployment in sidewall aneurysms, this additional section 222 also offers some advantages when used in bifurcation aneurysms as well. For instance, the proximal occlusive section 222 offers additional blood disruption at the proximal section of the device 210 toward the neck-portion of the aneurysm, thereby reducing blood flow into the aneurysm and promoting healing over time. Additionally, the articulation described above can be used to properly position the intrasaccular device 210 within a bifurcation aneurysm, for example in a particularly wide or large-necked aneurysm where it may be difficult to otherwise seat the intrasaccular device 210 properly with regard to the neck region of the aneurysm.

In some embodiments, the first occlusive element 240 and second occlusive element 222 comprise similar metallic wire material. In some embodiments, the first occlusive element 240 may be softer and have a more flexible configuration than the second occlusive element 222. More stiffness may be desirable along the proximal occlusive element 222 in order to provide enough push force against first occlusive element 240 and to provide more flow resistance along the proximal section of the intrasaccular implant 210. The first occlusive element 240, for instance, can use relatively smaller wires and/or a denser wind pattern than the second shell 222 in order to achieve this more flexible configuration. In contrast, the second occlusive element 222 may be stiffer than the first shell 240. This enhanced stiffness is achieved, for instance, by use of larger sized wires which are more spread out (e.g. having a smaller pic count). The second occlusive element 222 can also include radiopaque components, such as tantalum, to further enhance stiffness and well as to augment visualization. A good shape memory material, such as nitinol and/or DFT wire, may also be used to create the metallic mesh for the first 240 and second 222 occlusive elements.

The first occlusive element 240 may be formed by weaving or braiding between about 24 and 216 filaments, alternatively between about 60 and 144 filaments, alternatively between about 72 and 108 filaments. The filaments that are woven to form the first occlusive element 240 may have a diameter of between about 0.0005″ and 0.002″, alternatively between about 0.0006″ and 0.00125″, alternatively between about 0.00075″ and 0.001″. The first occlusive element 240 may have a radial stiffness between about 0.014 lbf and 0.284 lbf.

The second occlusive element 222 may be formed by weaving or braiding between about 24 and 216 filaments, alternatively between 60 and 144 filaments, alternatively between about 72 and 108 filaments. The filaments that are woven to form the second occlusive element 222 may have a diameter of between about 0.0005″ and 0.002″, alternatively between about 0.0006″ and 0.00125″, alternatively between about 0.00075″ and 0.001″. The second occlusive element 222 may have a radial stiffness between about 0.014 lbf and 0.284 lbf.

For some embodiments, the permeable shell 40, 140, 240 or portions thereof may be porous and may be highly permeable to liquids. In contrast to most vascular prosthesis fabrics or grafts which typically have a water permeability below 2,000 ml/min/cm² when measured at a pressure of 120 mmHg, the permeable shell 40 of some embodiments discussed herein may have a water permeability greater than about 2,000 ml/min/cm², in some cases greater than about 2,500 ml/min/cm². For some embodiments, water permeability of the permeable shell 40 or portions thereof may be between about 2,000 and 10,000 ml/min/cm², more specifically, about 2,000 ml/min/cm² to about 15,000 ml/min/cm², when measured at a pressure of 120 mmHg.

Device embodiments and components thereof may include metals, polymers, biologic materials and composites thereof. Suitable metals include zirconium-based alloys, cobalt-chrome alloys, nickel-titanium alloys, platinum, tantalum, stainless steel, titanium, gold, and tungsten. Potentially suitable polymers include but are not limited to acrylics, silk, silicones, polyvinyl alcohol, polypropylene, polyvinyl alcohol, polyesters (e.g. polyethylene terephthalate or PET), PolyEtherEther Ketone (PEEK), polytetrafluoroethylene (PTFE), polycarbonate urethane (PCU) and polyurethane (PU). Device embodiments may include a material that degrades or is absorbed or eroded by the body. A bioresorbable (e.g., breaks down and is absorbed by a cell, tissue, or other mechanism within the body) or bioabsorbable (similar to bioresorbable) material may be used. Alternatively, a bioerodable (e.g., erodes or degrades over time by contact with surrounding tissue fluids, through cellular activity or other physiological degradation mechanisms), biodegradable (e.g., degrades over time by enzymatic or hydrolytic action, or other mechanism in the body), or dissolvable material may be employed. Each of these terms is interpreted to be interchangeable. bioabsorbable polymer. Potentially suitable bioabsorbable materials include polylactic acid (PLA), poly(alpha-hydroxy acid) such as poly-L-lactide (PLLA), poly-D-lactide (PDLA), polyglycolide (PGA), polydioxanone, polycaprolactone, polygluconate, polylactic acid-polyethylene oxide copolymers, modified cellulose, collagen, poly(hydroxybutyrate), polyanhydride, polyphosphoester, poly(amino acids), or related copolymer materials. An absorbable composite fiber may be made by combining a reinforcement fiber made from a copolymer of about 18% glycolic acid and about 82% lactic acid with a matrix material consisting of a blend of the above copolymer with about 20% polycaprolactone (PCL).

Permeable shell embodiments 40, 140, 240 may be formed at least in part of wire, ribbon, or other filamentary elements. These filamentary elements 14 may have circular, elliptical, ovoid, square, rectangular, or triangular cross-sections. Permeable shell embodiments 40 may also be formed using conventional machining, laser cutting, electrical discharge machining (EDM) or photochemical machining (PCM). If made of a metal, it may be formed from either metallic tubes or sheet material.

Device embodiments 10, 110, 210 discussed herein may be delivered and deployed from a delivery and positioning system 112 that includes a microcatheter 61, such as the type of microcatheter 61 that is known in the art of neurovascular navigation and therapy. Device embodiments for treatment of a patient's vasculature 10, 110, 210 may be elastically collapsed and restrained by a tube or other radial restraint, such as an inner lumen 120 of a microcatheter 61, for delivery and deployment. The microcatheter 61 may generally be inserted through a small incision 152 accessing a peripheral blood vessel such as the femoral artery or brachial artery. The microcatheter 61 may be delivered or otherwise navigated to a desired treatment site 154 from a position outside the patient's body 156 over a guidewire 159 under fluoroscopy or by other suitable guiding methods. The guidewire 159 may be removed during such a procedure to allow insertion of the device 10, 110, 210 secured to a delivery apparatus 111 of the delivery system 112 through the inner lumen 120 of a microcatheter 61 in some cases. FIG. 17 illustrates a schematic view of a patient 158 undergoing treatment of a vascular defect 160 as shown in FIG. 18. An access sheath 162 is shown disposed within either a radial artery 164 or femoral artery 166 of the patient 158 with a delivery system 112 that includes a microcatheter 61 and delivery apparatus 111 disposed within the access sheath 162. The delivery system 112 is shown extending distally into the vasculature of the patient's brain adjacent a vascular defect 160 in the patient's brain.

Access to a variety of blood vessels of a patient may be established, including arteries such as the femoral artery 166, radial artery 164, and the like in order to achieve percutaneous access to a vascular defect 160. In general, the patient 158 may be prepared for surgery and the access artery is exposed via a small surgical incision 152 and access to the lumen is gained using the Seldinger technique where an introducing needle is used to place a wire over which a dilator or series of dilators dilates a vessel allowing an introducer sheath 162 to be inserted into the vessel. This would allow the device to be used percutaneously. With an introducer sheath 162 in place, a guiding catheter 168 is then used to provide a safe passageway from the entry site to a region near the target site 154 to be treated. For example, in treating a site in the human brain, a guiding catheter 168 would be chosen which would extend from the entry site 152 at the femoral artery up through the large arteries extending around the heart through the aortic arch, and downstream through one of the arteries extending from the upper side of the aorta such as the carotid artery 170. Typically, a guidewire 159 and neurovascular microcatheter 61 are then placed through the guiding catheter 168 and advanced through the patient's vasculature, until a distal end 151 of the microcatheter 61 is disposed adjacent or within the target vascular defect 160, such as an aneurysm. Exemplary guidewires 159 for neurovascular use include the Synchro2® made by Boston Scientific and the Glidewire Gold Neuro® made by MicroVention Terumo. Typical guidewire sizes may include 0.014 inches and 0.018 inches. Once the distal end 151 of the catheter 61 is positioned at the site, often by locating its distal end through the use of radiopaque marker material and fluoroscopy, the catheter is cleared. For example, if a guidewire 159 has been used to position the microcatheter 61, it is withdrawn from the catheter 61 and then the implant delivery apparatus 111 is advanced through the microcatheter 61.

Delivery and deployment of device embodiments 10, 110, 210 discussed herein may be carried out by first compressing the device 10, 110, 210 to a radially constrained and longitudinally flexible state as shown in FIG. 11. The device 10, 110, 210 may then be delivered to a desired treatment site 154 while disposed within the microcatheter 61, and then ejected or otherwise deployed from a distal end 151 of the microcatheter 61. In other method embodiments, the microcatheter 61 may first be navigated to a desired treatment site 154 over a guidewire 159 or by other suitable navigation techniques. The distal end of the microcatheter 61 may be positioned such that a distal port of the microcatheter 61 is directed towards or disposed within a vascular defect 160 to be treated and the guidewire 159 withdrawn. The device 10, 110, 210 secured to a suitable delivery apparatus 111 may then be radially constrained, inserted into a proximal portion of the inner lumen 120 of the microcatheter 61 and distally advanced to the vascular defect 160 through the inner lumen 120.

Once disposed within the vascular defect 160, the device 10, 110, 210 may then allowed to assume an expanded relaxed or partially relaxed state with the permeable shell 40, 140, 240 of the device spanning or partially spanning a portion of the vascular defect 160 or the entire vascular defect 160. The device 10, 110, 210 may also be activated by the application of an energy source to assume an expanded deployed configuration once ejected from the distal section of the microcatheter 61 for some embodiments. Once the device 10 is deployed at a desired treatment site 154, the microcatheter 61 may then be withdrawn.

Some embodiments of devices for the treatment of a patient's vasculature 10, 110, 210 discussed herein may be directed to the treatment of specific types of defects of a patient's vasculature. For example, referring to FIG. 18, an aneurysm 160 commonly referred to as a terminal aneurysm is shown in section. Terminal aneurysms occur typically at bifurcations in a patient's vasculature where blood flow, indicated by the arrows 172, from a supply vessel splits into two or more branch vessels directed away from each other. The main flow of blood from the supply vessel 174, such as a basilar artery, sometimes impinges on the vessel where the vessel diverges and where the aneurysm sack forms. Terminal aneurysms may have a well-defined neck structure where the profile of the aneurysm 160 narrows adjacent the nominal vessel profile, but other terminal aneurysm embodiments may have a less defined neck structure or no neck structure. FIG. 19 illustrates a typical berry type aneurysm 160 in section where a portion of a wall of a nominal vessel section weakens and expands into a sack like structure ballooning away from the nominal vessel surface and profile. Some berry type aneurysms may have a well-defined neck structure as shown in FIG. 19, but others may have a less defined neck structure or none at all. FIG. 19 also shows some optional procedures wherein a stent 173 or other type of support has been deployed in the parent vessel 174 adjacent the aneurysm. Also, shown is embolic material 176 being deposited into the aneurysm 160 through a microcatheter 61. Either or both of the stent 173 and embolic material 176 may be so deployed either before or after the deployment of a device for treatment of a patient's vasculature 10.

Prior to delivery and deployment of a device for treatment of a patient's vasculature 10, 110, 210, it may be desirable for the treating physician to choose an appropriately sized device 10, 110, 210 to optimize the treatment results. Some embodiments of treatment may include estimating a volume of a vascular site or defect 160 to be treated and selecting a device 10, 110, 210 with a volume that is substantially the same volume or slightly over-sized relative to the volume of the vascular site or defect 160. The volume of the vascular defect 160 to be occluded may be determined using three-dimensional angiography or other similar imaging techniques along with software which calculates the volume of a selected region. The amount of over-sizing may be between about 2% and 15% of the measured volume. In some embodiments, such as a very irregular shaped aneurysm, it may be desirable to under-size the volume of the device 10, 110, 210. Small lobes or “daughter aneurysms” may be excluded from the volume, defining a truncated volume which may be only partially filled by the device without affecting the outcome. A device 10, 110, 210 deployed within such an irregularly shaped aneurysm 160 is shown in FIG. 28 discussed below. Such a method embodiment may also include implanting or deploying the device 10, 110, 210 so that the vascular defect 160 is substantially filled volumetrically by a combination of device and blood contained therein. The device 10, 110, 210 may be configured to be sufficiently conformal to adapt to irregular shaped vascular defects 160 so that at least about 75%, in some cases about 80%, of the vascular defect volume is occluded by a combination of device 10, 110, 210 and blood contained therein.

In particular, for some treatment embodiments, it may be desirable to choose a device 10, 110, 210 that is properly oversized in a transverse dimension so as to achieve a desired conformance, radial force and fit after deployment of the device 10. FIGS. 20-22 illustrate a schematic representation of how a device 10, 110, 210 may be chosen for a proper fit after deployment that is initially oversized in a transverse dimension by at least about 10% of the largest transverse dimension of the vascular defect 160 and sometimes up to about 100% of the largest transverse dimension. For some embodiments, the device 10, 110, 210 may be oversized a small amount (e.g. less than about 1.5 mm) in relation to measured dimensions for the width, height or neck diameter of the vascular defect 160.

In FIG. 20, a vascular defect 160 in the form of a cerebral aneurysm is shown with horizontal arrows 180 and vertical arrows 182 indicating the approximate largest interior dimensions of the defect 160. Arrow 180 extending horizontally indicates the largest transverse dimension of the defect 160. In FIG. 21, a dashed outline 184 of a device for treatment of the vascular defect is shown superimposed over the vascular defect 160 of FIG. 20 illustrating how a device 10, 110, 210 that has been chosen to be approximately 20% oversized in a transverse dimension would look in its unconstrained, relaxed state. FIG. 22 illustrates how the device 10, 110, 210, which is indicated by the dashed line 184 of FIG. 21 might conform to the interior surface of the vascular defect 160 after deployment whereby the nominal transverse dimension of the device 10, 110, 210 in a relaxed unconstrained state has now been slightly constrained by the inward radial force 185 exerted by the vascular defect 160 on the device 10, 110, 210. In response, as the filaments 14, 114, 214 of the device 10, 110, 210 and thus the permeable shell 40, 140, 240 made therefrom have a constant length, the device 10, 110, 210 has assumed a slightly elongated shape in the axial or longitudinal axis of the device 10 so as to elongate and better fill the interior volume of the defect 160 as indicated by the downward arrow 186 in FIG. 22.

Once a properly sized device 10, 110, 210 has been selected, the delivery and deployment process may then proceed. It should also be noted also that the properties of the device embodiments 10, 110, 210 and delivery system embodiments 112 discussed herein generally allow for retraction of a device 10 after initial deployment into a defect 160, but before detachment of the device 10, 110, 210. Therefore, it may also be possible and desirable to withdraw or retrieve an initially deployed device 10 after the fit within the defect 160 has been evaluated in favor of a differently sized device 10, 110, 210. An example of a terminal aneurysm 160 is shown in FIG. 23 in section. The tip 151 of a catheter, such as a microcatheter 61 may be advanced into or adjacent the vascular site or defect 160 (e.g. aneurysm) as shown in FIG. 24. For some embodiments, an embolic coil or other vaso-occlusive device or material 176 (as shown for example in FIG. 19) may optionally be placed within the aneurysm 160 to provide a framework for receiving the device 10, 110, 210. In addition, a stent 173 may be placed within a parent vessel 174 of some aneurysms substantially crossing the aneurysm neck prior to or during delivery of devices for treatment of a patient's vasculature discussed herein (also as shown for example in FIG. 19). An example of a suitable microcatheter 61 having an inner lumen diameter of about 0.020 inches to about 0.022 inches is the Rapid Transit® manufactured by Cordis Corporation. Examples of some suitable microcatheters 61 may include microcatheters having an inner lumen diameter of about 0.026 inch to about 0.028 inch, such as the Rebar® by Ev3 Company, the Renegade Hi-Flow® by Boston Scientific Corporation, and the Mass Transit® by Cordis Corporation. Suitable microcatheters having an inner lumen diameter of about 0.031 inch to about 0.033 inch may include the Marksmen® by Chestnut Medical Technologies, Inc. and the Vasco 28® by Balt Extrusion. A suitable microcatheter 61 having an inner lumen diameter of about 0.039 inch to about 0.041 inch includes the Vasco 35 by Balt Extrusion. These microcatheters 61 are listed as exemplary embodiments only, other suitable microcatheters may also be used with any of the embodiments discussed herein.

Detachment of the device 10, 110, 210 from the delivery apparatus 111 may be controlled by a control switch 188 disposed at a proximal end of the delivery system 112, which may also be coupled to an energy source 142, which severs the tether 72 that secures the proximal hub 68 of the device 10 to the delivery apparatus 111. While disposed within the microcatheter 61 or other suitable delivery system 112, as shown in FIG. 11, the filaments 14, 114, 214 of the permeable shell 40, 140, 240 may take on an elongated, non-everted configuration substantially parallel to each other and a longitudinal axis of the catheter 61. Once the device 10, 110, 210 is pushed out of the distal port of the microcatheter 61, or the radial constraint is otherwise removed, the distal ends 62 of the filaments 14, 114, 214 may then axially contract towards each other so as to assume the globular everted configuration within the vascular defect 160 as shown in FIG. 25.

The device 10, 110, 210 may be inserted through the microcatheter 61 such that the catheter lumen 120 restrains radial expansion of the device 10, 110, 210 during delivery. Once the distal tip or deployment port of the delivery system 112 is positioned in a desirable location adjacent or within a vascular defect 160, the device 10, 110, 210 may be deployed out the distal end of the catheter 61 thus allowing the device to begin to radially expand as shown in FIG. 25. As the device 10, 110, 210 emerges from the distal end of the delivery system 112, the device 10, 110, 210 expands to an expanded state within the vascular defect 160, but may be at least partially constrained by an interior surface of the vascular defect 160.

Upon full deployment, radial expansion of the device 10, 110, 210 may serve to secure the device 10, 110, 210 within the vascular defect 160 and also deploy the permeable shell 40 across at least a portion of an opening 190 (e.g. aneurysm neck) so as to at least partially isolate the vascular defect 160 from flow, pressure or both of the patient's vasculature adjacent the vascular defect 160 as shown in FIG. 26. The conformability of the device 10, 110, 210, particularly in the neck region 190 may provide for improved sealing. For some embodiments, once deployed, the permeable shell 40, 140, 240 may substantially slow the flow of fluids and impede flow into the vascular site and thus reduce pressure within the vascular defect 160. For some embodiments, the device 10, 110, 210 may be implanted substantially within the vascular defect 160, however, in some embodiments, a portion of the device 10, 110, 210 may extend into the defect opening or neck 190 or into branch vessels.

For some embodiments, as discussed above, the device 10, 110, 210 may be manipulated by the user to position the device 10, 110, 210 within the vascular site or defect 160 during or after deployment but prior to detachment. For some embodiments, the device 10, 110, 210 may be rotated in order to achieve a desired position of the device 10 and, more specifically, a desired position of the permeable shell 40, 140, 240, 340, 440, prior to or during deployment of the device 10, 110, 210. For some embodiments, the device 10, 110, 210 may be rotated about a longitudinal axis of the delivery system 112 with or without the transmission or manifestation of torque being exhibited along a middle portion of a delivery catheter being used for the delivery. It may be desirable in some circumstances to determine whether acute occlusion of the vascular defect 160 has occurred prior to detachment of the device 10, 110, 210 from the delivery apparatus 111 of the delivery system 112. These delivery and deployment methods may be used for deployment within berry aneurysms, terminal aneurysms, or any other suitable vascular defect embodiments 160. Some method embodiments include deploying the device 10, 110, 210 at a confluence of three vessels of the patient's vasculature that form a bifurcation such that the permeable shell 40 of the device 10, 110, 210 substantially covers the neck of a terminal aneurysm. Once the physician is satisfied with the deployment, size and position of the device 10, 110, 210, the device 10, 110, 210 may then be detached by actuation of the control switch 188 by the methods described above and shown in FIG. 26. Thereafter, the device 10, 110, 210 is in an implanted state within the vascular defect 160 to effect treatment thereof.

FIG. 27 illustrates another configuration of a deployed and implanted device in a patient's vascular defect 160. While the implantation configuration shown in FIG. 26 indicates a configuration whereby the longitudinal axis 46 of the device 10, 110, 210 is substantially aligned with a longitudinal axis of the defect 160, other suitable and clinically effective implantation embodiments may be used. For example, FIG. 27 shows an implantation embodiment whereby the longitudinal axis 46 of the implanted device 10, 110, 210 is canted at an angle of about 10 degrees to about 90 degrees relative to a longitudinal axis of the target vascular defect 160. Such an alternative implantation configuration may also be useful in achieving a desired clinical outcome with acute occlusion of the vascular defect 160 in some cases and restoration of normal blood flow adjacent the treated vascular defect. FIG. 28 illustrates a device 10, 110, 210 implanted in an irregularly shaped vascular defect 160. The aneurysm 160 shown has at least two distinct lobes 192 extending from the main aneurysm cavity. The two lobes 192 shown are unfilled by the deployed vascular device 10, 110, 210, yet the lobes 192 are still isolated from the parent vessel of the patient's body due to the occlusion of the aneurysm neck portion 190.

Markers, such as radiopaque markers, on the device 10, 110, 210 or delivery system 112 may be used in conjunction with external imaging equipment (e.g. x-ray) to facilitate positioning of the device or delivery system during deployment. Once the device is properly positioned, the device 10 may be detached by the user. For some embodiments, the detachment of the device 10, 110, 210 from the delivery apparatus 111 of the delivery system 112 may be affected by the delivery of energy (e.g. heat, radiofrequency, ultrasound, vibrational, or laser) to a junction or release mechanism between the device 10 and the delivery apparatus 111. Once the device 10, 110, 210 has been detached, the delivery system 112 may be withdrawn from the patient's vasculature or patient's body 158. For some embodiments, a stent 173 may be place within the parent vessel substantially crossing the aneurysm neck 190 after delivery of the device 10 as shown in FIG. 19 for illustration.

For some embodiments, a biologically active agent or a passive therapeutic agent may be released from a responsive material component of the device 10, 110, 210. The agent release may be affected by one or more of the body's environmental parameters or energy may be delivered (from an internal or external source) to the device 10, 110, 210. Hemostasis may occur within the vascular defect 160 as a result of the isolation of the vascular defect 160, ultimately leading to clotting and substantial occlusion of the vascular defect 160 by a combination of thrombotic material and the device 10, 110, 210. For some embodiments, thrombosis within the vascular defect 160 may be facilitated by agents released from the device 10 and/or drugs or other therapeutic agents delivered to the patient.

For some embodiments, once the device 10, 110, 210 has been deployed, the attachment of platelets to the permeable shell 40 may be inhibited and the formation of clot within an interior space of the vascular defect 160, device, or both promoted or otherwise facilitated with a suitable choice of thrombogenic coatings, anti-thrombogenic coatings or any other suitable coatings (not shown) which may be disposed on any portion of the device 10, 110, 210 for some embodiments, including an outer surface of the filaments 14 or the hubs 66 and 68. Such a coating or coatings may be applied to any suitable portion of the permeable shell 40. Energy forms may also be applied through the delivery apparatus 111 and/or a separate catheter to facilitate fixation and/or healing of the device 10, 110, 210 adjacent the vascular defect 160 for some embodiments. One or more embolic devices or embolic material 176 may also optionally be delivered into the vascular defect 160 adjacent permeable shell portion that spans the neck or opening 190 of the vascular defect 160 after the device 10 has been deployed. For some embodiments, a stent or stent-like support device 173 may be implanted or deployed in a parent vessel adjacent the defect 160 such that it spans across the vascular defect 160 prior to or after deployment of the vascular defect treatment device 10, 110, 210.

In any of the above embodiments, the device 10, 110, 210 may have sufficient radial compliance so as to be readily retrievable or retractable into a typical microcatheter 61. The proximal portion of the device 10, 110, 210, or the device as a whole for some embodiments, may be engineered or modified by the use of reduced diameter filaments, tapered filaments, or filaments oriented for radial flexure so that the device 10, 110, 210 is retractable into a tube that has an internal diameter that is less than about 0.7 mm, using a retraction force less than about 2.7 Newtons (0.6 lbf) force. The force for retrieving the device 10, 110, 210 into a microcatheter 61 may be between about 0.8 Newtons (0.18 lbf) and about 2.25 Newtons (0.5 lbf).

Engagement of the permeable shell 40, 140, 240 with tissue of an inner surface of a vascular defect 160, when in an expanded relaxed state, may be achieved by the exertion of an outward radial force against tissue of the inside surface of the cavity of the patient's vascular defect 160, as shown for example in FIG. 29. A similar outward radial force may also be applied by a proximal end portion and permeable shell 40, 140, 240 of the device 10, 110, 210 so as to engage the permeable shell 40 with an inside surface or adjacent tissue of the vascular defect 160. Such forces may be exerted in some embodiments wherein the nominal outer transverse dimension or diameter of the permeable shell 40 in the relaxed unconstrained state is larger than the nominal inner transverse dimension of the vascular defect 160 within which the device 10, 110, 210 is being deployed, i.e., oversizing as discussed above. The elastic resiliency of the permeable shell 40 and filaments 14 thereof may be achieved by an appropriate selection of materials, such as superelastic alloys, including nickel titanium alloys, or any other suitable material for some embodiments. The conformability of a proximal portion of the permeable shell 40, 140, 240 of the device 10, 110, 210 may be such that it will readily ovalize to adapt to the shape and size of an aneurysm neck 190, as shown in FIGS. 20-22, thus providing a good seal and barrier to flow around the device. Thus, the device 10 may achieve a good seal, substantially preventing flow around the device without the need for fixation members that protrude into the parent vessel.

Although the foregoing invention has, for the purposes of clarity and understanding, been described in some detail by way of illustration and example, it will be obvious that certain changes and modifications may be practiced which will still fall within the scope of the appended claims. 

1. A device for treatment of a patient's cerebral aneurysm, comprising: a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the expanded state of the second permeable shell is configured to sit within the recessed section of the first permeable shell, wherein the proximal end of the first permeable shell is coupled with the distal end of the second permeable shell.
 2. The device of claim 1, wherein the recessed section is concave in shape.
 3. The device of claim 2, wherein the expanded state of the second permeable shell further contains a distal convex section at the distal end of the second permeable shell, wherein the distal convex section is configured to receive the elongate proximal extension of the first permeable shell.
 4. The device of claim 1, wherein the first and second permeable shells are formed from the same plurality of filaments.
 5. The device of claim 1, wherein the plurality of filaments forming the first permeable shell is different from the plurality of filaments forming the second permeable shell.
 6. The device of claim 1, further comprising a proximal hub attached to a proximal end of the second permeable shell.
 7. The device of claim 1, further comprising a distal hub attached to a distal end of the first permeable shell.
 8. The device of claim 1, wherein a proximal end of the second permeable shell is coupled to a pusher.
 9. A cerebral sidewall aneurysm treatment device, comprising: a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the distal end of the second permeable shell is coupled to the proximal end of the first permeable shell, and wherein the proximal end of the second permeable shell is coupled with a delivery pusher, wherein the second permeable shell is configured to exert force against the recessed section of the first permeable shell in order to position the first permeable shell over a neck region of the cerebral sidewall aneurysm.
 10. The device of claim 9, wherein the first permeable shell further comprises an elongate proximal extension having a proximal end, wherein the proximal end of the elongate proximal extension sits within the recessed section.
 11. The device of claim 10, wherein the first permeable shell further comprises an elongate distal extension and a distal concave section, wherein at least a portion of the elongate distal extension sits within the distal concave section of the first permeable shell.
 12. The device of claim 11, wherein the elongate distal extension is longer than the elongate proximal extension of the first permeable shell.
 13. The device of claim 10, wherein the first permeable shell and second permeable shell are coupled through the elongate proximal extension.
 14. The device of claim 10, wherein the elongate proximal extension is a wire braid.
 15. The device of claim 10, wherein the elongate proximal extension allows for the first permeable shell to deflect at an angle relative to a longitudinal axis of the second permeable shell.
 16. The device of claim 10, wherein a length of the elongate proximal extension is smaller than a height of the recessed section.
 17. The device of claim 9, wherein the first permeable shell is capable of deflecting relative to a longitudinal axis formed by the pusher and the second permeable shell.
 18. The device of claim 15, wherein the first permeable shell is capable of deflecting at an angle up to about 180° relative to a longitudinal axis formed by the pusher and the second permeable shell.
 19. A device for treatment of a patient's cerebral aneurysm, comprising: a first permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, the expanded state having a proximal end with a recessed section adapted to sit over a neck of an aneurysm; and a second permeable shell having a proximal end, a distal end, a radially constrained elongated state configured for delivery within a catheter lumen, an expanded state with a longitudinally shortened configuration relative to the radially constrained state, and a plurality of elongate filaments that are woven together to form a mesh, wherein the distal end of the second permeable shell is coupled with the proximal end of the first permeable shell, wherein the second permeable shell is configured to occupy the recessed section of the first permeable shell to augment surface coverage over the neck of the aneurysm.
 20. The device of claim 19, wherein the second permeable shell does not extend proximally past a plane defined by the proximal most edge of the first permeable shell when the first permeable shell is in the expanded state and the second permeable shell is in its expanded state whereby it is configured to occupy the recessed section of the first permeable shell. 21-40. (canceled) 